Clinical Research Coordinator III – Infectious Diseases

Emory University

. Independently manage significant and key aspects of a large clinical trial or all aspects of one or more small trials or research projects .

Posted 10/12/2026full-timeAtlanta • United StatesJuniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical trials, including participant recruitment, data management, and compliance with regulations. Proficient in clinical procedures such as phlebotomy and specimen collection, with a strong focus on leadership and process improvement.

Highest-signal resume keywords

Clinical Trial ManagementData ManagementParticipant Recruitment StrategiesPhlebotomyCertified Research Administrator

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ExperienceData ManagementPhlebotomySpecimen CollectionGrant Proposal DevelopmentProtocol AuthoringIRB Submission MonitoringCompliance AuditingCorrective Action ImplementationLaboratory Procedure Oversight

Soft Skills

LeadershipTraining and GuidanceProblem SolvingCommunicationSupervisory Skills

Certifications & Qualifications

Certified Research AdministratorClinical Research Coordinator

Industry Keywords

Clinical TrialsResearch ProtocolsParticipant RetentionSAE ReportingClinical Researcher CredentialingHealth Related ProgramsRegulatory ComplianceResearch Participant InteractionLaboratory OperationsClinical Patient Contact

About the role

Key responsibilities & impact

Independently manage significant and key aspects of a large clinical trial or all aspects of one or more small trials or research projects
Train and provide guidance to less experienced staff
Oversee data management for research projects
Interface with research participants and resolve issues related to study protocols
Authorize purchases for supplies and equipment maintenance
Determine effective strategies for promoting and recruiting research participants and retaining participants in long-term clinical trials
Periodically audit operations, including laboratory procedures, to ensure compliance with applicable regulations
Provide leadership in identifying and implementing corrective actions and processes
Monitor IRB submissions and respond to requests and questions
Interface with study sponsors and monitors, report SAEs, and resolve study queries
Provide leadership in determining, recommending, and implementing improvements to policies and processes
Assist in developing grant proposals and protocols
Perform phlebotomy, specimen collection, or diagnostics with appropriate credentialing and training
Perform some supervisory duties
Perform related approved responsibilities as required

Requirements

What you’ll need

High School Diploma or GED and seven years of clinical research experience
Or two years of college in a scientific, health related or business administration program and five years of clinical research experience
Or licensed as a Practical Nurse (LPN) and four years of clinical research experience
Or bachelor's degree in a scientific, health related or business administration program and three years clinical research experience
Or master's degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience
Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred
Clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher
Position involves clinical patient contact and potential exposure to hazardous chemicals, human blood, body fluids, tissues, or other potentially infectious materials

Benefits

Comp & perks

Equal opportunity employment
Reasonable accommodations for qualified individuals with disabilities
Participation in university programs and use of facilities without discrimination